CN112251912B - Capparis spinosa drug-loaded nanofiber membrane as well as preparation method and application thereof - Google Patents
Capparis spinosa drug-loaded nanofiber membrane as well as preparation method and application thereof Download PDFInfo
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/70—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres
- D04H1/72—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged
- D04H1/728—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged by electro-spinning
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
- D01F1/103—Agents inhibiting growth of microorganisms
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- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/88—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
- D01F6/92—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyesters
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- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
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- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4326—Condensation or reaction polymers
- D04H1/435—Polyesters
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- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/005—Synthetic yarns or filaments
- D04H3/009—Condensation or reaction polymers
- D04H3/011—Polyesters
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- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/02—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of forming fleeces or layers, e.g. reorientation of yarns or filaments
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- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
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- D10B2509/00—Medical; Hygiene
- D10B2509/02—Bandages, dressings or absorbent pads
- D10B2509/022—Wound dressings
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Abstract
The invention relates to a caper drug-loaded nanofiber membrane as well as a preparation method and application thereof, and belongs to the field of preparation of drug-loaded nanofibers. The caper drug-loaded nanofiber membrane is prepared by mixing a polylactic acid solution and an caper ethyl acetate extract to obtain a spinning solution and performing electrostatic spinning. The caper ethyl acetate extract is prepared by the following method: carrying out reflux purification on the caper fruit powder by using absolute ethyl alcohol under a water bath kettle at 60 ℃; filtering, collecting supernatant, diluting the obtained supernatant with water, extracting with isovolumetric petroleum ether for several times, adding sodium chloride during extraction, separating the solution into three layers, taking the lowest layer solution, continuously adding isovolumetric ethyl acetate for extraction, taking the lower layer solution after the solution is layered, and concentrating to obtain the caper ethyl acetate extract. The fiber membrane of the invention has antibacterial property, good hydrophilicity and good moisture permeability.
Description
Technical Field
The invention relates to a caper drug-loaded nanofiber membrane as well as a preparation method and application thereof, belonging to the field of preparation of drug-loaded nanofibers.
Background
The electrostatic spinning technology is a special fiber manufacturing process realized under the condition of high voltage, liquid drops at a needle head of a polymer solution or a melt are changed into a cone shape (namely a Taylor cone) from a spherical shape under the condition of high voltage, nano-scale to micron-scale fibers are obtained by extending from the tip of the cone, and finally a nano-fiber film is obtained on a receiving device. Because of the advantages of simple production equipment, low manufacturing cost, various spinnable varieties, controllable process and the like, the electrostatic spinning technology has become a main approach for preparing the nanofiber material. At present, the technology has potential application value in the fields of biological materials, filtration and protection, wound dressing, food engineering and the like. The drug-loaded nanofiber membrane prepared by the electrostatic spinning technology has the advantages of high specific surface area, high aperture ratio and high moisture permeability, is favorable for cell proliferation and adhesion, and can provide a good environment for wound repair.
Polylactic acid (PLA) is a novel biodegradable material with good mechanical properties. In addition, PLA has good biocompatibility, moisture permeability, air permeability and nontoxicity, and polylactic acid can be decomposed into monomer lactic acid, and a human body also contains lactic acid existing in a monomer form, so that the PLA material is harmless to the human body and has potential application value in the field of medical use.
Capparis spinosa L is a Capparis plant of Capparidaceae Capparis, is called wild watermelon in China, is mainly distributed in the middle east and Mediterranean countries, and is mainly distributed in Sinkiang, gansu, tibet and other areas in China. The root bark, the leaves and the fruits of the Chinese medicinal composition can be used as medicines, and have wide application in China. The fruits of Han nationality, uyghur nationality and Kataer nationality are mainly used for treating various rheumatism, eliminating phlegm, stopping spasm, relieving pain, etc. Modern pharmacological research shows that the caper fruit extract has certain effects in bacteriostasis, anti-inflammation, antioxidation and the like. However, no report on the preparation of the caper ethyl acetate extract nanofiber membrane by using the electrospinning technology exists at present.
Disclosure of Invention
The invention aims to solve the technical problem of providing the caper ethyl acetate extract-loaded nanofiber membrane and the preparation method thereof.
The caper drug-loaded nanofiber membrane is prepared by mixing a polylactic acid solution and an caper ethyl acetate extract to obtain a spinning solution and performing electrostatic spinning.
The caper ethyl acetate extract is in the form of extract.
The caper drug-loaded nanofiber membrane is a nanofiber membrane loaded with an caper ethyl acetate extract component, and the caper ethyl acetate extract effective component is uniformly distributed in fibers; the drug-loaded nanofiber membrane is a drug-loaded PLA nanofiber membrane.
The caper drug-loaded nanofiber membrane disclosed by the invention is a hydrophilic fiber membrane.
The diameter of the fiber in the caper drug-loaded nanofiber membrane is 206.2 +/-6.37 nm.
The caper drug-loaded nanofiber membrane disclosed by the invention has antibacterial activity, and further has antibacterial activity on escherichia coli or staphylococcus aureus.
The caper ethyl acetate extract is prepared by the following method: carrying out reflux purification on the caper fruit powder by using absolute ethyl alcohol under a water bath kettle at 60 ℃; filtering, collecting supernatant, diluting the supernatant with water, extracting with isovolumetric petroleum ether for several times, adding sodium chloride during the extraction process, dividing the solution into three layers, taking the lowest layer solution, continuously adding isovolumetric ethyl acetate for extraction, taking the lower layer solution after the solution is layered, and concentrating to obtain the caper ethyl acetate extract.
Preferably, the method for preparing the caper ethyl acetate extract comprises the following steps: pulverizing the caper fruit by using a pulverizer to prepare powder of 40 meshes. 100g of caper powder was purified by refluxing with 600mL of absolute ethanol in a 60 ℃ water bath for 3 times (2 h/time), filtered using a Buchner funnel and the supernatant collected, and concentrated by a vacuum rotary evaporator. And (3) concentrating the supernatant to 25mL, adding 75mL of distilled water, extracting the mixed solution for three times by using isometric petroleum ether, adding 0.5g of sodium chloride in the extraction process, dividing the solution into three layers, taking the solution at the lowest layer, continuously adding isometric ethyl acetate for extraction, taking the solution at the lower layer after the solution is layered, and concentrating by using a vacuum rotary evaporator to obtain the final product, namely the caper ethyl acetate extract.
Preferably, the mass percentage concentration of the polylactic acid in the polylactic acid solution is 5-8%, and the used solvent is a mixture of trichloromethane and acetone according to the mass ratio of 2: 1.
Preferably, the mass percentage concentration of the caper ethyl acetate extract in the spinning solution is 4% -10%.
Preferably, the electrostatic spinning process parameters are as follows: the specification of the injector is 20mL, the specification of the pillow is 21G, the flow rate of the spinning solution is 0.3-1mL/h, the voltage is 13-18kV, the receiving distance is 12-15cm, the spinning time is 8-10h, and aluminum foil collection is carried out; the electrostatic spinning environment temperature is 30 ℃, and the spinning humidity is 35-40%.
The invention also aims to provide a preparation method of the caper ethyl acetate extract.
A preparation method of caper drug-loaded nanofiber membrane comprises the following process steps:
(1) Dissolving polylactic acid in a solvent to obtain a polylactic acid solution;
(2) Adding the caper ethyl acetate extract into the polylactic acid solution, stirring and dissolving to obtain a spinning solution, then performing electrostatic spinning, and drying to obtain the caper drug-loaded nanofiber membrane.
Preferably, the preparation method of the caper drug-loaded nanofiber membrane comprises the following steps: dissolving PLA powder in a chloroform/acetone (2: 1, w/w) mixed solution, adding an caper ethyl acetate extract to obtain a spinning solution, performing electrostatic spinning, and drying in a vacuum drying oven at 25 ℃ for 12-24 hours to obtain the caper drug-loaded nanofiber membrane.
Preferably, the mass percentage concentration of the polylactic acid in the polylactic acid solution is 5-8%, and the used solvent is a mixture of trichloromethane and acetone according to the mass ratio of 2: 1.
Preferably, the mass percentage concentration of the caper ethyl acetate extract in the spinning solution is 4% -10%.
Preferably, the electrostatic spinning process parameters are as follows: the specification of the injector is 20mL, the specification of the pillow is 21G, the flow rate of the spinning solution is 0.3-1mL/h, the voltage is 13-18kV, the receiving distance is 12-15cm, the spinning time is 8-10h, and aluminum foil collection is carried out; the electrostatic spinning environment temperature is 30 ℃, and the spinning humidity is 35-40%.
Further, the electrostatic spinning step specifically comprises: pouring the spinning solution into an injector, fixing the injector on an electrostatic spinning device, and adjusting spinning technological parameters to carry out electrostatic spinning. The electrostatic spinning environment temperature is 30 ℃, the spinning humidity is 35-40%, the flow rate of the spinning solution is 0.3-1mL/h, the voltage is 13-18kV, the receiving distance is 12-15cm, the spinning time is 8-10h, and the aluminum foil is adhered to a roller collector.
Preferably, the stirring dissolution temperature in the step (2) is 35 ℃, and the stirring time is 6-12h.
Preferably, the drying in the step (2) is carried out in a vacuum drying oven at the temperature of 25 ℃ for 12-24h.
The invention also aims to provide application of the caper drug-loaded nanofiber membrane as a medical dressing.
Further, the medical dressing is a medical wound dressing.
The invention has the beneficial effects that: (1) The preparation method is simple and feasible, and the obtained fiber has small and uniform diameter and high specific surface area and is suitable for the field of biological medical treatment. (2) The fiber film of the invention has antibacterial property, good hydrophilicity and good moisture permeability.
Drawings
FIGS. 1 (a) and (b) are SEM image (a) and histogram of diameter distribution (b), respectively, of the drug-free PLA film of example 1;
fig. 2 (a) and (b) are SEM image (a) and histogram of diameter distribution (b), respectively, of the drug-loaded PLA film of example 2;
FIGS. 3 (a) - (c) show the contact angles of the non-loaded PLA film of example 3 at 5s, 10s, and 15s, respectively;
FIGS. 4 (a) - (c) show the contact angles of the drug-loaded PLA film of example 4 at 5s, 10s, and 15s, respectively;
FIGS. 5 (a) and (b) are the inhibition zones of the PLA films described in examples 1, 2, 5, 6, respectively, for Escherichia coli (a) and Staphylococcus aureus (b).
Detailed Description
The invention will be further illustrated with reference to the following specific examples. It should be understood that these examples are for illustrative purposes only and are not intended to limit the scope of the present invention. Further, it should be understood that various changes or modifications of the present invention can be made by those skilled in the art after reading the teaching of the present invention, and these equivalents also fall within the scope of the claims appended to the present application.
The performance test of the drug-loaded nanofiber membrane disclosed by the invention comprises the following steps:
(1) Contact angle testing: the nanofiber membranes tested were cut into strips (2 cm x3 cm), the strip-like fiber membranes were fixed horizontally on a glass slide, 2. Mu.L of distilled water was dropped on the fiber membranes, and the change in contact angle was recorded after they were contacted for 5s, 10s, 15 s.
(2) And (3) antibacterial testing: shearing nanofiber membranes with different drug-loading concentrations (0%, 4%, 7% and 10%) and the diameters of the nanofiber membranes are 6mm, and placing the nanofiber membranes on solid culture media containing different bacteria for an antibacterial test; the bacteria are respectively selected from Escherichia coli and Staphylococcus aureus.
(3) Moisture permeability test: shearing a circular nanofiber membrane with the diameter of 70mm, and testing the moisture absorption performance of the drug-loaded nanofiber membrane by using a wet absorption method under the conditions that the temperature is 38 ℃, the relative humidity is 90% and the air flow rate is 0.3-05 m/s.
The potential of applying the drug-loaded PLA to the wound dressing is determined through testing the contact angle, the antibiosis and the moisture permeability of the drug-loaded nanofiber membrane.
The method for preparing the caper ethyl acetate extract described in the following examples is as follows: the caper fruit is crushed by a crusher to prepare 40-mesh powder. 100g of caper powder was purified by refluxing with 600mL of absolute ethanol in a 60 ℃ water bath for 3 times (2 h/time), filtered using a Buchner funnel and the supernatant collected, and concentrated by a vacuum rotary evaporator. And (3) concentrating the supernatant to 25mL, adding 75mL of distilled water, extracting the mixed solution for three times by using isometric petroleum ether, adding 0.5g of sodium chloride in the extraction process, dividing the solution into three layers, taking the solution at the lowest layer, continuously adding isometric ethyl acetate to extract, taking the solution at the lower layer after the solution is layered, and concentrating by using a vacuum rotary evaporator to obtain the final product, namely the caper ethyl acetate extract.
Example 1
(1) 0.6g of PLA was weighed and dissolved in 9.4g of a chloroform/acetone (2: 1, w/w) mixed solution, and the mixture was magnetically stirred for 12 hours until the solute was completely dissolved in the solvent, thereby obtaining a PLA spinning solution.
(2) And pouring the spinning solution into a 20mL syringe, fixing the syringe on an electrostatic spinning device, and adjusting spinning process parameters to carry out electrostatic spinning. The electrostatic spinning environment temperature is 30 ℃, the spinning humidity is 38%, the flow rate of the spinning solution is 0.8mL/h, the voltage is 15kV, the receiving distance is 13cm, the spinning time is 9h, and the aluminum foil is adhered to a roller collector to obtain the PLA nanofiber membrane without drug loading.
(3) And (3) putting the PLA nanofiber membrane without the drug loading into a vacuum drying oven at 25 ℃, and drying for 15h to obtain the dried PLA nanofiber membrane.
(4) According to the steps, the PLA nanofiber membrane without drug loading is obtained, SEM tests show as figure 1 show that the fiber surface is smooth and has no bead-shaped structure, and analysis on fiber diameter distribution by using image J software shows that the fiber diameter distribution is uniform, and the average fiber diameter is 284.28nm.
Example 2
(1) 0.6g of PLA was weighed out and dissolved in 8.4g of a chloroform/acetone (2: 1, w/w) mixed solution.
(2) Adding 1g of caper ethyl acetate extract into the solution, and magnetically stirring for 12 hours at 35 ℃ until the solute is completely dissolved in the solvent to obtain the PLA spinning solution with 10% of caper ethyl acetate extract.
(3) Pouring the spinning solution into a 20mL injector, fixing the injector on an electrostatic spinning device, adjusting spinning process parameters to perform electrospinning, wherein the ambient temperature of electrostatic spinning is 30 ℃, the spinning humidity is 38%, the flow rate of the spinning solution is 0.8mL/h, the voltage is 15kV, the receiving distance is 13cm, the spinning time is 9h, and aluminum foil is adhered to a roller collector to obtain the PLA nanofiber membrane with 10% of the caper ethyl acetate extract.
(4) And (3) putting the nanofiber membrane into a vacuum drying oven at 25 ℃, and drying for 15h to obtain the dried PLA nanofiber membrane with 10% of the caper ethyl acetate extract.
(5) According to the steps, the PLA nanofiber membrane with the ponkan ethyl acetate extract content of 10% is obtained, SEM tests show that fibers have no bead-shaped structure, the fiber diameter distribution is uniform, slight adhesion occurs at nodes, concave-convex feeling exists on the fiber surface, and analysis of the fiber diameter distribution by using image J software shows that the average diameter of the PLA nanofiber membrane with the ponkan ethyl acetate extract content of 10% is 206.20nm, the diameter of the nanofibers after drug loading is reduced, and slight adhesion and concave-convex unevenness occur on the fiber surface.
Example 3
(1) 0.6g of PLA was weighed and dissolved in 9.4g of a chloroform/acetone (2: 1, w/w) mixed solution, and the mixture was magnetically stirred for 12 hours until the solute was completely dissolved in the solvent, thereby obtaining a PLA spinning solution.
(2) Pouring the spinning solution into a 20mL injector, fixing the injector on an electrostatic spinning device, adjusting spinning process parameters to perform electrospinning, wherein the ambient temperature of electrostatic spinning is 30 ℃, the spinning humidity is 38%, the flow rate of the spinning solution is 0.8mL/h, the voltage is 15kV, the acceptance distance is 13cm, the spinning time is 9h, and an aluminum foil is adhered to a roller collector to obtain the drug-free PLA nanofiber membrane.
(3) And (3) putting the PLA nanofiber membrane without the drug loading into a vacuum drying oven at 25 ℃, and drying for 15h to obtain the dried PLA nanofiber membrane.
(4) The nanofiber membrane was cut into strips (2 cmx3 cm), the strip-shaped fiber membranes were horizontally fixed on a glass slide, 2. Mu.L of distilled water was dropped on the fiber membranes, and the change of contact angle was recorded after they were contacted for 5s, 10s, and 15s, as shown in FIG. 3. The contact angle of the PLA nanofiber membrane without drug loading is larger, the contact angle after 15s is 137.1 +/-0.2 degrees, the PLA nanofiber membrane belongs to a hydrophobic material, and the electrostatic spinning technology can be known to not change the hydrophobic property of the PLA material.
Example 4
(1) 0.6g of PLA was weighed out and dissolved in 8.4g of a chloroform/acetone (2: 1, w/w) mixed solution.
(2) Adding 1g of caper ethyl acetate extract into the solution, and magnetically stirring for 12 hours at the temperature of 35 ℃ until solute is completely dissolved in the solvent to obtain a PLA spinning solution containing 10% of the caper ethyl acetate extract.
(3) Pouring the spinning solution into a 20mL injector, fixing the injector on an electrostatic spinning device, adjusting spinning process parameters to perform electrospinning, wherein the ambient temperature of electrostatic spinning is 30 ℃, the spinning humidity is 38%, the flow rate of the spinning solution is 0.8mL/h, the voltage is 15kV, the receiving distance is 13cm, the spinning time is 9h, and aluminum foil is adhered to a roller collector to obtain the PLA nanofiber membrane with 10% of the caper ethyl acetate extract.
(4) And (3) putting the nanofiber membrane into a vacuum drying oven at 25 ℃, and drying for 15 hours to obtain the PLA nanofiber membrane with the dried caper ethyl acetate extract content of 10%.
(5) The nanofiber membrane described above was cut into strips (2 cmx3 cm), the strip-shaped fiber membrane was horizontally fixed on a glass slide, 2. Mu.L of distilled water was dropped on the fiber membrane, and changes in contact angle were recorded after they were contacted for 5s, 10s, and 15s, as shown in FIG. 4. Compared with a PLA nanofiber membrane without a medicament, the PLA nanofiber membrane with the 10% of caper ethyl acetate extract is obviously reduced in contact angle and enhanced in material hydrophilicity, the contact angle after 15s is 24.1 +/-5 degrees and is changed into a hydrophilic material, the hydrophilicity of the material is mainly changed by adding the caper ethyl acetate extract, and a good environment is created for wound healing when the caper ethyl acetate extract is used for wound dressing.
Example 5
(1) 0.6g of PLA was weighed out and dissolved in 9g of a chloroform/acetone (2: 1, w/w) mixed solution.
(2) Adding 0.4g of caper ethyl acetate extract into the solution, and magnetically stirring for 12 hours at 35 ℃ until solute is completely dissolved in the solvent to obtain the PLA spinning solution with the caper ethyl acetate extract content of 4%.
(3) Pouring the spinning solution into a 20mL injector, fixing the injector on an electrostatic spinning device, adjusting spinning process parameters to perform electrospinning, wherein the ambient temperature of electrostatic spinning is 30 ℃, the spinning humidity is 38%, the flow rate of the spinning solution is 0.8mL/h, the voltage is 15kV, the receiving distance is 13cm, the spinning time is 9h, and aluminum foil is adhered to a roller collector to obtain the PLA nanofiber membrane with the ponkan ethyl acetate extract content of 4%.
(4) And (3) putting the nanofiber membrane into a vacuum drying oven at 25 ℃, and drying for 15h to obtain the dried PLA nanofiber membrane with the caper ethyl acetate extract content of 4%.
Example 6
(1) 0.6g of PLA was weighed out and dissolved in 8.7g of a chloroform/acetone (2: 1, w/w) mixed solution.
(2) Adding 0.7g of caper ethyl acetate extract into the solution, and magnetically stirring for 12 hours at the temperature of 35 ℃ until solute is completely dissolved in the solvent to obtain a PLA spinning solution containing the caper ethyl acetate extract with the concentration of 7%.
(3) Pouring the spinning solution into a 20mL injector, fixing the injector on an electrostatic spinning device, adjusting spinning process parameters to perform electrospinning, wherein the ambient temperature of electrostatic spinning is 30 ℃, the spinning humidity is 38%, the flow rate of the spinning solution is 0.8mL/h, the voltage is 15kV, the receiving distance is 13cm, the spinning time is 9h, and aluminum foil is adhered to a roller collector to obtain the PLA nanofiber membrane with the caper ethyl acetate extract content of 7%.
(4) And (3) putting the nanofiber membrane into a vacuum drying oven at 25 ℃, and drying for 15 hours to obtain the PLA nanofiber membrane with the dried caper ethyl acetate extract content of 7%.
(5) The dried fiber membranes of the embodiments 3, 4, 5 and 6 are respectively taken, the nanofiber membranes with different drug-loading concentrations (0%, 4%, 7% and 10%) and diameters of 6mm are cut, the aluminum foil is removed, the fiber membranes are respectively placed on solid culture media which are pre-coated with escherichia coli and staphylococcus aureus and cultured for 15 hours in an incubator at 37 ℃, as shown in fig. 5, the nanofiber membranes with different drug-loading rates have different bacteriostatic rings on the escherichia coli and the staphylococcus aureus, and the obtained drug-loading nanofiber membranes have good bacteriostatic effects and great potential in the application aspect of medical dressings.
Example 7
The dried nanofiber membranes of examples 3 and 4 were taken, and circular nanofiber membranes with a diameter of 70mm were cutAnd respectively testing the moisture absorption performance of the nano fiber membrane without drug loading and the moisture absorption performance of the nano fiber membrane with drug loading by adopting a moisture absorption method under the conditions of 38 ℃ of temperature, 90% of relative humidity and 0.3-0.5m/s of air flow speed. Experiments are carried out according to the national standard GB/T12704-91 moisture permeable cup method for measuring the moisture permeability of fabrics. The moisture permeability of the nano fiber membrane without drug loading is 5783.64 g/(m) 2 D), and the moisture permeability of the PLA nanofiber membrane with the drug loading of 10 percent is 7181.59 g/(m) 2 D), the moisture permeability is significantly increased. The prepared drug-loaded nanofiber membrane can provide a good environment for wound healing.
Claims (8)
1. The caper drug-loaded nanofiber membrane is characterized in that the drug-loaded nanofiber membrane is obtained by carrying out electrostatic spinning on a spinning solution obtained by mixing a polylactic acid solution and an caper ethyl acetate extract; the caper ethyl acetate extract is prepared by the following method: carrying out reflux purification on the caper fruit powder by using absolute ethyl alcohol under a water bath kettle at 60 ℃; filtering, collecting supernatant, diluting the obtained supernatant with water, extracting with isovolumetric petroleum ether for several times, adding sodium chloride during extraction, separating the solution into three layers, taking the lowest layer solution, continuously adding isovolumetric ethyl acetate for extraction, taking the lower layer solution after the solution is layered, and concentrating to obtain the caper ethyl acetate extract.
2. The nanofiber membrane as claimed in claim 1, wherein the mass percentage concentration of polylactic acid in the polylactic acid solution is 5% -8%, and the used solvent is a mixture of chloroform and acetone according to a mass ratio of 2:1, in a mixture of the components.
3. The nanofiber membrane as claimed in claim 1, wherein the ethyl acetate caper extract is present in the spinning solution in a mass percentage of 4% -10%.
4. The nanofiber membrane of claim 1, wherein the electrospinning process parameters are: the specification of the injector is 20mL, the specification of the pillow is 21G, the flow rate of the spinning solution is 0.3-1mL/h, the voltage is 13-18kV, the receiving distance is 12-15cm, the spinning time is 8-10h, and aluminum foil collection is carried out; the electrostatic spinning environment temperature is 30 ℃, and the spinning humidity is 35-40%.
5. The preparation method of the caper drug-loaded nanofiber membrane as claimed in claim 1, which is characterized by comprising the following process steps:
(1) Dissolving polylactic acid in a solvent to obtain a polylactic acid solution;
(2) Adding the caper ethyl acetate extract into the polylactic acid solution, stirring and dissolving to obtain a spinning solution, then performing electrostatic spinning, and drying to obtain the caper drug-loaded nanofiber membrane.
6. The method as claimed in claim 5, wherein the stirring dissolution temperature in the step (2) is 35 ℃ and the stirring time is 6-12h.
7. The method as set forth in claim 5, wherein the drying in the step (2) is carried out in a vacuum drying oven at a temperature of 25 ℃ for a drying time of 12 to 24 hours.
8. The use of the caper drug-loaded nanofiber membrane of claim 1 as a medical dressing.
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